Adrenocorticotropic Hormone for Childhood Nephrotic Syndrome: The ATLANTIS Randomized Trial

dc.contributor.authorWang, Chia-shi
dc.contributor.authorTravers, Curtis
dc.contributor.authorMcCracken, Courtney
dc.contributor.authorLeong, Traci
dc.contributor.authorGbadegesin, Rasheed
dc.contributor.authorQuiroga, Alejandro
dc.contributor.authorBenfield, Mark R.
dc.contributor.authorHidalgo, Guillermo
dc.contributor.authorSrivastava, Tarak
dc.contributor.authorLo, Megan
dc.contributor.authorYadin, Ora
dc.contributor.authorMathias, Robert
dc.contributor.authorAraya, Carlos E.
dc.contributor.authorKhalid, Myda
dc.contributor.authorOrjuela, Alvaro
dc.contributor.authorZaritsky, Joshua
dc.contributor.authorAl-Akash, Samhar
dc.contributor.authorKamel, Margret
dc.contributor.authorGreenbaum, Larry A.
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2020-03-19T18:38:50Z
dc.date.available2020-03-19T18:38:50Z
dc.date.issued2018-12-07
dc.description.abstractBackground and objectives There is renewed interest in adrenocorticotropic hormone (ACTH) for the treatment of nephrotic syndrome. We evaluated the efficacy and safety of ACTH in children with frequently relapsing or steroid-dependent nephrotic syndrome in a randomized trial. Design, setting, participants, & measurements Participants aged 2–20 years old with frequently relapsing or steroid-dependent nephrotic syndrome were enrolled from 16 sites in the United States and randomized 1:1 to ACTH (repository corticotropin injection) or no relapse-preventing treatment. ACTH treatment regimen was 80 U/1.73 m2 administered twice weekly for 6 months, followed by 40 U/1.73 m2 administered twice weekly for 6 months. The primary outcome was disease relapse during the first 6 months. Participants in the control group were offered crossover to ACTH treatment if they relapsed within 6 months. Secondary outcomes were relapse after ACTH dose reduction and treatment side effects. Results The trial was stopped at a preplanned interim analysis after enrollment of 31 participants because of a lack of discernible treatment efficacy. Fourteen out of 15 (93%) participants in the ACTH arm experienced disease relapse in the first 6 months, with a median time to first relapse of 23 days (interquartile range, 9–32), compared with 15 out of 16 (94%) participants and at a median of 21 days (interquartile range, 14–51) in the control group. There was no difference in the proportion of relapsed patients (odds ratio, 0.93; 95% confidence interval, 0.05 to 16.40; P>0.99) or time to first relapse (hazard ratio, 1.03; 95% confidence interval, 0.50 to 2.15; P=0.93). Thirteen out of 16 participants in the control group crossed over to ACTH treatment. Three out of 28 participants completed 12 months of ACTH treatment; the others exited the trial because of frequent relapses or side effects. There were no disease relapses after ACTH dose reduction among the three participants. Most side effects were mild and similar to side effects of corticosteroids. Conclusions ACTH at 80 U/1.73 m2 administered twice weekly was ineffective at preventing disease relapses in pediatric nephrotic syndrome.en_US
dc.identifier.citationWang, C. S., Travers, C., McCracken, C., Leong, T., Gbadegesin, R., Quiroga, A., ... & Yadin, O. (2018). Adrenocorticotropic hormone for childhood nephrotic syndrome: the ATLANTIS randomized trial. Clinical Journal of the American Society of Nephrology, 13(12), 1859-1865. 10.2215/CJN.06890618en_US
dc.identifier.issn1555-9041, 1555-905Xen_US
dc.identifier.urihttps://hdl.handle.net/1805/22382
dc.language.isoen_USen_US
dc.publisherAmerican Society of Nephrologyen_US
dc.relation.isversionof10.2215/CJN.06890618en_US
dc.relation.journalClinical Journal of the American Society of Nephrologyen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectNephrotic syndromeen_US
dc.subjectClinical trialen_US
dc.subjectChildrenen_US
dc.subjectAdrenocorticotropic Hormoneen_US
dc.subjectChildhood Nephrotic Syndromeen_US
dc.titleAdrenocorticotropic Hormone for Childhood Nephrotic Syndrome: The ATLANTIS Randomized Trialen_US
dc.typeArticleen_US
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302334/en_US
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